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Strychnos usambarensis

Strychnos usambarensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644004bbb2662520387732
Scientific name Strychnos usambarensis
Authority Gilg ex Engl.
First published in Abh. Königl. Akad. Wiss. Berlin 1894: 36 (1894)

Description Top

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Synonyms Top

Scientific name Authority First published in
Strychnos cerasifera Gilg Pflanzenw. Ost-Afrikas , C: 311 (1895)
Strychnos distichophylla Gilg Pflanzenw. Ost-Afrikas , C: 310 (1895)

Common names Top

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Language Common/alternative name
Afrikaans bloubitterbessie

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Burundi
      • Congo
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000501270
Tropicos 19000634
KEW urn:lsid:ipni.org:names:547543-1
The Plant List kew-2595082
Open Tree Of Life 455165
NCBI Taxonomy 992791
IPNI 547543-1
iNaturalist 340209
GBIF 5645098
Freebase /m/0wbhqhq
EOL 5345304
USDA GRIN 417573
Wikipedia Strychnos_usambarensis

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Drug target of natural products and COVID-19: how far has science progressed? Raman K, Rajagopal K, Ramesh B, Nallasivan PK, Raja MK, Jupudi S, Byran G, Khan SL, Bin Emran T Ann Med Surg (Lond) 19-Apr-2023
PMCID:PMC10289732
doi:10.1097/MS9.0000000000000703
PMID:37363478
Plant Molecular Pharming and Plant-Derived Compounds towards Generation of Vaccines and Therapeutics against Coronaviruses Venkataraman S Vaccines (Basel) 26-Oct-2022
PMCID:PMC9699630
doi:10.3390/vaccines10111805
PMID:36366313
Unveiling antiplasmodial alkaloids from a cumulative collection of Strychnos extracts by multi-informative molecular networks Bonnet O, Beniddir MA, Champy P, Degotte G, Mamede L, Desdemoustier P, Ledoux A, Tchinda AT, Angenot L, Frédérich M Front Mol Biosci 26-Sep-2022
PMCID:PMC9548993
doi:10.3389/fmolb.2022.967012
PMID:36225255
Development of spiro-3-indolin-2-one containing compounds of antiproliferative and anti-SARS-CoV-2 properties Fawazy NG, Panda SS, Mostafa A, Kariuki BM, Bekheit MS, Moatasim Y, Kutkat O, Fayad W, El-Manawaty MA, Soliman AA, El-Shiekh RA, Srour AM, Barghash RF, Girgis AS Sci Rep 16-Aug-2022
PMCID:PMC9380671
doi:10.1038/s41598-022-17883-9
PMID:35974029
The naturally‐derived alkaloids as a potential treatment for COVID‐19: A scoping review Gonzalez BL, de Oliveira NC, Ritter MR, Tonin FS, Melo EB, Sanches AC, Fernandez‐Llimos F, Petruco MV, de Mello JC, Chierrito D, de Medeiros Araújo DC Phytother Res 30-Mar-2022
PMCID:PMC9111026
doi:10.1002/ptr.7442
PMID:35355337
Inhibitory effects of selected isoquinoline alkaloids against main protease (Mpro) of SARS-CoV-2, in silico study Sadeghi M, Miroliaei M In Silico Pharmacol 14-Mar-2022
PMCID:PMC8918422
doi:10.1007/s40203-022-00122-4
PMID:35310017
Alkaloids and Colon Cancer: Molecular Mechanisms and Therapeutic Implications for Cell Cycle Arrest Khan H, Alam W, Alsharif KF, Aschner M, Pervez S, Saso L Molecules 28-Jan-2022
PMCID:PMC8838632
doi:10.3390/molecules27030920
PMID:35164185
Biological Activity of Naturally Derived Naphthyridines Chabowska G, Barg E, Wójcicka A Molecules 16-Jul-2021
PMCID:PMC8306249
doi:10.3390/molecules26144324
PMID:34299599
Anti-ovarian cancer potential of phytocompound and extract from South African medicinal plants and their role in the development of chemotherapeutic agents Palanisamy CP, Cui B, Zhang H, Panagal M, Paramasivam S, Chinnaiyan U, Jeyaraman S, Murugesan K, Rostagno M, Sekar V, Natarajan SP Am J Cancer Res 15-May-2021
PMCID:PMC8167668
PMID:34094656
A review on potential of natural products in the management of COVID-19 Chakravarti R, Singh R, Ghosh A, Dey D, Sharma P, Velayutham R, Roy S, Ghosh D RSC Adv 12-May-2021
PMCID:PMC9031656
doi:10.1039/d1ra00644d
PMID:35479175
Alkaloids and flavonoids from African phytochemicals as potential inhibitors of SARS-Cov-2 RNA-dependent RNA polymerase: an in silico perspective Ogunyemi OM, Gyebi GA, Elfiky AA, Afolabi SO, Ogunro OB, Adegunloye AP, Ibrahim IM Antivir Chem Chemother 29-Dec-2020
PMCID:PMC7783895
doi:10.1177/2040206620984076
PMID:33372806
In Silico Identification of New Targets for Diagnosis, Vaccine, and Drug Candidates against Trypanosoma cruzi Trevisan RO, Santos MM, Desidério CS, Alves LG, de Jesus Sousa T, de Castro Oliveira L, Jaiswal AK, Tiwari S, Bovi WG, de Oliveira-Silva M, Costa-Madeira JC, Castellano LR, Silva MV, Azevedo V, Rodrigues Junior V, Oliveira CJ, de Castro Soares S Dis Markers 10-Dec-2020
PMCID:PMC7787821
doi:10.1155/2020/9130719
PMID:33488847
Phytochemicals: Potential Therapeutic Interventions Against Coronavirus-Associated Lung Injury Majnooni MB, Fakhri S, Shokoohinia Y, Kiyani N, Stage K, Mohammadi P, Gravandi MM, Farzaei MH, Echeverría J Front Pharmacol 18-Nov-2020
PMCID:PMC7919380
doi:10.3389/fphar.2020.588467
PMID:33658931
Indole: The After Next Scaffold of Antiplasmodial Agents? Surur AS, Huluka SA, Mitku ML, Asres K Drug Des Devel Ther 11-Nov-2020
PMCID:PMC7666986
doi:10.2147/DDDT.S278588
PMID:33204071
Prevention of SARS-CoV-2 cell entry: insight from in silico interaction of drug-like alkaloids with spike glycoprotein, human ACE2, and TMPRSS2 Gyebi GA, Adegunloye AP, Ibrahim IM, Ogunyemi OM, Afolabi SO, Ogunro OB J Biomol Struct Dyn 22-Oct-2020
PMCID:PMC7594191
doi:10.1080/07391102.2020.1835726
PMID:33089728

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
(2R,3E,12bS)-2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-ylmethyl)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 135485580 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NCCC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(2R,3R,12bS)-3-ethyl-11-[(2S)-1-methylpyrrolidin-2-yl]-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,7a,12,12a,12b-decahydroindolo[2,3-a]quinolizin-10-ol 44559861 Click to see CCC1CN2CCC3C(C2CC1CC4C5=C(CCN4C)C6=CC=CC=C6N5)NC7=C3C=CC(=C7C8CCCN8C)O 553.80 unknown https://doi.org/10.1021/NP020070E
(2R,3Z,12bR)-3-ethylidene-2-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 163186006 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 432.60 unknown https://doi.org/10.1055/S-0028-1099529
(2S,12bS)-3-ethenyl-11-[(2R)-1-methylpyrrolidin-2-yl]-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 101967022 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1016/S0031-9422(00)81453-3
https://doi.org/10.1016/0009-2797(91)90025-3
(2S,12bS)-3-ethenyl-11-[(2S)-1-methylpyrrolidin-2-yl]-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 101624708 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1016/S0031-9422(00)81453-3
(2S,3R,12bS)-3-ethenyl-2-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-11-ol 163194833 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=C(N5)C(=CC=C6)O)NC7=CC=CC=C27 466.60 unknown https://doi.org/10.1055/S-0030-1264493
(2S,3Z,12bS)-2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-ylmethyl)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 163186547 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NCCC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://doi.org/10.1055/S-0028-1099529
(3R,6'R,7'R,8'aS)-6'-ethenyl-6-hydroxy-7-[(2R)-1-methylpyrrolidin-2-yl]-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163189724 Click to see CN1CCCC1C2=C(C=CC3=C2NC(=O)C34CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 565.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(3R,6'R,7'R,8'aS)-6'-ethenyl-6-hydroxy-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 21123429 Click to see CN1CCC2=C(C1CC3CC4C5(CCN4CC3C=C)C6=C(C=C(C=C6)O)NC5=O)NC7=CC=CC=C27 482.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(3S,6'R,7'R,8'aS)-6'-ethenyl-6-hydroxy-7-[(2R)-1-methylpyrrolidin-2-yl]-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163189725 Click to see CN1CCCC1C2=C(C=CC3=C2NC(=O)C34CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 565.70 unknown https://doi.org/10.1055/S-0030-1264493
(3S,6'R,7'S,8'aS)-6'-ethenyl-6-hydroxy-7'-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163185902 Click to see CN1CCC2=C(C1CC3CC4C5(CCN4CC3C=C)C6=C(C=C(C=C6)O)NC5=O)NC7=CC=CC=C27 482.60 unknown https://doi.org/10.1055/S-0030-1264493
1-[(3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl)methyl]-9H-pyrido[3,4-b]indol-6-ol 75072021 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=C5C=C(C=C6)O)NC7=CC=CC=C37 448.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1021/NP9804738
10-Hydroxydihydrousambarine 49863342 Click to see CCC1CN2CCC3=C(C2CC1CC4C5=C(CCN4C)C6=CC=CC=C6N5)NC7=C3C=C(C=C7)O 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
10-Hydroxyusambarensine 10433813 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=C5C=C(C=C6)O)NC7=CC=CC=C37 448.60 unknown https://doi.org/10.1021/NP980375M
https://doi.org/10.1021/NP9804738
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
10-Hydroxyusambarine 3084873 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=C(N5)C=CC(=C6)O)NC7=CC=CC=C27 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
10'-Hydroxyusambarensine 44566377 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=C5C=C(C=C6)O)NC7=CC=CC=C37 448.60 unknown https://doi.org/10.1021/NP980375M
11-Hydroxydihydrousambarine 49863369 Click to see CCC1CN2CCC3=C(C2CC1CC4C5=C(CCN4C)C6=CC=CC=C6N5)NC7=C3C=CC(=C7)O 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
11-Hydroxyusambarine 401427 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=C(N5)C=C(C=C6)O)NC7=CC=CC=C27 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
2-(4,9-dihydro-3H-pyrido[3,4-b]indol-1-ylmethyl)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 162987964 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NCCC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 434.60 unknown https://doi.org/10.1055/S-0028-1099529
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-11-(1-methylpyrrolidin-2-yl)-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 124977 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1055/S-0030-1264493
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/0009-2797(91)90025-3
https://doi.org/10.1016/S0031-9422(00)81453-3
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 78182284 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=C(N5)C=C(C=C6)O)NC7=CC=CC=C27 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-11-ol 163063236 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=C(N5)C(=CC=C6)O)NC7=CC=CC=C27 466.60 unknown https://doi.org/10.1055/S-0030-1264493
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-ol 78302558 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=C(N5)C=CC(=C6)O)NC7=CC=CC=C27 466.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethenyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine 5089095 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=CC=CC=C6N5)NC7=CC=CC=C27 450.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/S0031-9422(00)94682-X
3-Ethyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-10-ol 75309077 Click to see CCC1CN2CCC3=C(C2CC1CC4C5=C(CCN4C)C6=CC=CC=C6N5)NC7=C3C=CC(=C7)O 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-Ethyl-2-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-9-ol 75309071 Click to see CCC1CN2CCC3=C(C2CC1CC4C5=C(CCN4C)C6=CC=CC=C6N5)NC7=C3C=C(C=C7)O 468.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
3-ethylidene-2-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 6825683 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 432.60 unknown https://doi.org/10.1055/S-0028-1099529
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
6'-ethenyl-6-hydroxy-7-(1-methylpyrrolidin-2-yl)-7'-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 163024264 Click to see CN1CCCC1C2=C(C=CC3=C2NC(=O)C34CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 565.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-0030-1264493
6'-ethenyl-6-hydroxy-7'-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]spiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-2-one 155297 Click to see CN1CCC2=C(C1CC3CC4C5(CCN4CC3C=C)C6=C(C=C(C=C6)O)NC5=O)NC7=CC=CC=C27 482.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-0030-1264493
Dihydrousambarensine 136099744 Click to see CC=C1CN2CCC3C(C2CC1CC4=NCCC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 436.60 unknown https://doi.org/10.1021/NP020070E
Harmalan 160510 Click to see CC1=NCCC2=C1NC3=CC=CC=C23 184.24 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Isostrychnopentamine A 6712642 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1016/S0031-9422(00)81453-3
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1055/S-0030-1264493
Strychnopentamine 6712640 Click to see CN1CCCC1C2=C(C=CC3=C2NC4=C3CCN5C4CC(C(C5)C=C)CC6C7=C(CCN6C)C8=CC=CC=C8N7)O 549.70 unknown https://doi.org/10.1055/S-0030-1264493
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/S0031-9422(00)81453-3
Usambarensine 5281413 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 432.60 unknown https://doi.org/10.1021/NP980375M
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1021/NP020070E
https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Usambarine 442121 Click to see CN1CCC2=C(C1CC3CC4C5=C(CCN4CC3C=C)C6=CC=CC=C6N5)NC7=CC=CC=C27 450.60 unknown https://doi.org/10.1016/S0031-9422(00)94682-X
https://doi.org/10.1021/NP020070E
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
> Alkaloids and derivatives / Strychnos alkaloids
(1R,11S,12R,13R,14E,19S,21S)-14-ethylidene-10-[(2S,3E)-3-ethylidene-2,4-dihydro-1H-indolo[2,3-a]quinolizin-2-yl]-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-11-ol 163192960 Click to see CC=C1CN2CCC34C2CC1C5C3N(C=C(C5O)C6CC7=C8C(=C9C=CC=CC9=N8)C=CN7CC6=CC)C1=CC=CC=C41 566.70 unknown https://doi.org/10.1016/S0031-9422(97)00944-8
tetradehydrolongicaudatine Y 44559870 Click to see CC=C1CN2CCC3=C(C2CC1C4=CN5C6C(C4O)C7CC8C6(CCN8CC7=CCO)C9=CC=CC=C95)NC1=CC=CC=C31 586.80 unknown https://doi.org/10.1021/NP020070E
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
CID 11969719 11969719 Click to see CC=C(C=O)C1CC2C3=C(CCN2C)C4=CC=CC=C4N3C(C1)O 324.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Indolo(2',3':3,4)pyrido(1,2-b)(2,7)naphthyridinium, 5,7,8,13,13b,14-hexahydro-5,6-dimethyl-, (5S,6R,13bS)- 157739 Click to see CC1C2=C(CC3[N+]1(CCC4=C3NC5=CC=CC=C45)C)C=CN=C2 304.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9
Isomalindine 134716669 Click to see CC1C2=C(CC3[N+]1(CCC4=C3NC5=CC=CC=C45)C)C=CN=C2 304.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199803/04)9:2<63::AID-PCA388>3.0.CO;2-9

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